Label: MOTION SICKNESS RELIEF- meclizine hcl tablet
- NDC Code(s): 55910-943-19
- Packager: DOLGENCORP, LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated April 19, 2024
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredient (in each tablet)
- Purpose
- Uses
-
Warnings
Ask a doctor before use if you have
- glaucoma
- difficulty in urination due to enlargement of the prostate gland
- a breathing problem such as emphysema or chronic bronchitis
- glaucoma
- Directions
- Other information
- Inactive ingredients
- Questions or comments?
-
Principal Display Panel
DG™ | health
Compare to the
active ingredient
of Dramamine®
Less Drowsy*Less Drowsy Formula
Motion Sickness
ReliefMeclizine HCl 25 mg / Antiemetic
• Up to 24 hours of protection
• Prevents nausea , dizziness & vomiting
• Ages 12 Years and Over8 Tablets
Actual Tablet Size
25
mg eachTAMPER EVIDENT: DO NOT USE IF
PACKAGE IS OPENED OR IF BLISTER
UNIT IS TORN, BROKEN OR SHOWS
ANY SIGNS OF TAMPERINGDISTRIBUTED BY
OLD EAST MAIN CO.
100 MISSION RIDGE
GOODLETTSVILLE, TN 37072100%
Satisfaction
Guaranteed
(888)-309-9030*This product is not manufactured or distributed by Medtech
Products Inc., owner of the registered trademark
Dramamine® Less Drowsy. 50844 ORG042340319Dollar General 44-403A
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INGREDIENTS AND APPEARANCE
MOTION SICKNESS RELIEF
meclizine hcl tabletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:55910-943 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MECLIZINE HYDROCHLORIDE (UNII: HDP7W44CIO) (MECLIZINE - UNII:3L5TQ84570) MECLIZINE HYDROCHLORIDE 25 mg Inactive Ingredients Ingredient Name Strength SILICON DIOXIDE (UNII: ETJ7Z6XBU4) D&C YELLOW NO. 10 ALUMINUM LAKE (UNII: CQ3XH3DET6) LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X) MAGNESIUM STEARATE (UNII: 70097M6I30) STARCH, CORN (UNII: O8232NY3SJ) Product Characteristics Color yellow Score no score Shape ROUND Size 9mm Flavor Imprint Code 44;403 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:55910-943-19 1 in 1 CARTON 06/01/2019 1 8 in 1 BLISTER PACK; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M009 06/01/2019 Labeler - DOLGENCORP, LLC (068331990) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 038154464 pack(55910-943) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 832867837 manufacture(55910-943) , pack(55910-943) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 967626305 pack(55910-943) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 117025878 manufacture(55910-943)